Molecular-channel driven actuator with considerations for multiple configurations and color switchingJiuke Mu, Gang Wang, Hongping Yan et al.|Nature Communications|2018 The ability to achieve simultaneous intrinsic deformation with fast response in commercially available materials that can safely contact skin continues to be an unresolved challenge for artificial actuating materials. Rather than using a microporous structure, here we show an ambient-driven actuator that takes advantage of inherent nanoscale molecular channels within a commercial perfluorosulfonic acid ionomer (PFSA) film, fabricated by simple solution processing to realize a rapid response, self-adaptive, and exceptionally stable actuation. Selective patterning of PFSA films on an inert soft substrate (polyethylene terephthalate film) facilitates the formation of a range of different geometries, including a 2D (two-dimensional) roll or 3D (three-dimensional) helical structure in response to vapor stimuli. Chemical modification of the surface allowed the development of a kirigami-inspired single-layer actuator for personal humidity and heat management through macroscale geometric design features, to afford a bilayer stimuli-responsive actuator with multicolor switching capability.
Photopolymer Materials and Processes for Advanced TechnologiesPhotopolymers broadly comprise monomers, oligomers, polymers, or mixtures of the aforementioned materials that upon exposure to light undergo photochemical reactions that result in deep-seated changes in their structures which substantially modify their chemical and mechanical properties. Photopolymers may possess chromophores that provide for their intrinsic photosensitivity. Alternatively, other photosensitive molecules may be added that directly or indirectly interact with the photopolymer upon exposure to light to produce the desired property changes. Examples of various types of photopolymers will be presented in this article along with examples of their use in representative applications.
Chemical amplification mechanisms for microlithographyADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTChemical amplification mechanisms for microlithographyE. Reichmanis, F. M. Houlihan, O. Nalamasu, and T. X. NeenanCite this: Chem. Mater. 1991, 3, 3, 394–407Publication Date (Print):May 1, 1991Publication History Published online1 May 2002Published inissue 1 May 1991https://pubs.acs.org/doi/10.1021/cm00015a009https://doi.org/10.1021/cm00015a009research-articleACS PublicationsRequest reuse permissionsArticle Views1383Altmetric-Citations179LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Polymer materials for microlithographyADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPolymer materials for microlithographyElsa Reichmanis and Larry F. ThompsonCite this: Chem. Rev. 1989, 89, 6, 1273–1289Publication Date (Print):September 1, 1989Publication History Published online1 May 2002Published inissue 1 September 1989https://pubs.acs.org/doi/10.1021/cr00096a001https://doi.org/10.1021/cr00096a001research-articleACS PublicationsRequest reuse permissionsArticle Views2050Altmetric-Citations135LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Elastomer–Polymer Semiconductor Blends for High-Performance Stretchable Charge Transport NetworksDalsu Choi, Hyungchul Kim, Nils Persson et al.|Chemistry of Materials|2016 An inverse relationship between mechanical ductility and mobility/molecular ordering in conjugated polymer systems was determined definitively through systematic interrogation of poly(3-hexylthiophene) (P3HT) films with varied degrees of molecular ordering and associated charge transport performance. The dilemma, whereby molecular ordering required for efficient charge transport conclusively undermines the applicability of these materials for stretchable, flexible device applications, was resolved using a polymer blend approach. Specifically, the molecular interactions between dissimilar polymer materials advantageously induced semiconducting polymer ordering into efficient π–π stacked fibrillar networks. Changes in the molecular environment surrounding the conjugated polymer during the elastomer curing process further facilitated development of high mobility networked semiconductor pathways. A processed P3HT: poly(dimethylsiloxane) (PDMS) composite afforded a semiconducting film that exhibits superior ductility and notable mobility versus the single-component polymer semiconductor counterpart.